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6F3N

Crystal structure of S-adenosyl-L-homocysteine hydrolase from Pseudomonas aeruginosa cocrystallized with SAH in the presence of K+ and Zn2+ cations

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.3
Synchrotron siteBESSY
Beamline14.3
Temperature [K]100
Detector technologyCCD
Collection date2014-12-06
DetectorRAYONIX MX-225
Wavelength(s)0.8950
Spacegroup nameC 1 2 1
Unit cell lengths170.585, 99.275, 111.721
Unit cell angles90.00, 101.90, 90.00
Refinement procedure
Resolution24.820 - 1.850
R-factor0.15136
Rwork0.151
R-free0.17648
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.014
RMSD bond angle1.599
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0155)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0001.920
High resolution limit [Å]1.8501.850
Rmerge0.082
Number of reflections152489
<I/σ(I)>10.2
Completeness [%]98.3
Redundancy2.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP29250 mM KH2PO4, 20% (w/v) PEG8000, 1 mM S-adenosyl-L-homocysteine

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